Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive fragility and photosensitivity disorder Kindler syndrome

• ASHTON GHS

収録刊行物

• J Invest Dermatol

  J Invest Dermatol 122 78-83, 2004

詳細情報

• CRID: 1571980075974296832
• NII論文ID: 30014542019
• DOI: 10.1046/j.0022-202x.2003.22136.x
• データソース種別:
  • CiNii Articles